drugset / Trial / NCT07219459

Visugromab, Nivolumab and Lenvatinib Compared to Double Placebo and Lenvatinib in Unresectable or Metastatic Hepatocellular Carcinoma Post Anti-PD-(L)1 Failure

NCT07219459

Phase 2 Recruiting 104 enrolled CatalYm GmbH
RandomizedParallel-groupTriple-blindTreatment

Summary

This is a Phase 2b, randomized, blinded clinical trial investigating the efficacy and safety of visugromab in combination with nivolumab and Lenvatinib compared to double placebo and Lenvatinib in participants with unresectable or metastatic HCC and compensated liver function (Child-Pugh A) after failure of 1L treatment that included an anti-PD-(L)1 compound. The trial consists of 2 Parts: a non-randomized Safety-run-in part (Part 1) and the subsequent randomized part (Part 2) with 2 treatment arms (A and B). Randomization of participants into Treatment Arm A and B will continue until 40 efficacy-evaluable participants are enrolled into each Treatment Arm.

Timeline

Start
2026-03-19
Primary completion
2029-09
Completion
2031-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Nivolumab Monoclonal antibody 360 mg Intravenous
Subject Visugromab Monoclonal antibody Intravenous
Background Lenvatinib Small molecule 8 mg Oral
Background Lenvatinib Small molecule 12 mg Oral